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我父亲肺鳞癌的治疗贴(2014年3月1日驾鹤西去)

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1346937 1620 老马 发表于 2011-10-27 08:05:18 | 置顶 |
老马  博士一年级 发表于 2012-4-27 18:50:42 | 显示全部楼层 来自: 浙江温州
Pooled Analysis of S-1 Trials in Non-Small Cell Lung Cancer According to Histological Type8 g# d1 S$ U6 N* G6 C
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
8 G( r% d7 m* U& Q+ Author Affiliations
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4 Q+ M, B+ f' D6 O& Z1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
7 n" I( X& _& \4 O, J! y  _9 c2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan " Q# z1 q3 j. ~3 T/ q
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan ( h# }7 P! L- F# ~
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan 6 |9 \- W8 Z- \
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
. I: g/ K3 o+ }+ I6 d1 K- i6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
5 u) w1 Y! J0 \4 x7Kinki University School of Medicine, Osaka 589-8511, Japan
: i# [( C# M5 i4 U* L+ a' ?/ X9 {+ S. f8Izumi Municipal Hospital, Osaka 594-0071, Japan
$ p3 {2 z& e3 d" O9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
3 _" i# x0 W: _Correspondence to: Nobuyuki Yamamoto, Division of Thoracic Oncology, Shizuoka Cancer Center, 1007 Shimonagakubo, Nagaizumi-cho, Sunto-gun, Shizuoka 411-8777, Japan. Tel: +81 559895222, Fax: +81 559895783, e-mail: n.yamamoto@scchr.jp
, }) A: e1 j; c+ o$ L5 T+ S- u; k; DAbstractBackground: The antimetabolic agent S-1 inhibits thymidylate synthase similar to pemetrexed, but through a different mechanism of action. Whether the antitumour activity of S-1 depends on histological type remains unclear. We analysed pooled data from 2 phase II clinical studies of cisplatin and S-1 in patients with previously untreated advanced non-small cell lung cancer. Patients and Methods: We comprised 110 patients with stage IIIB or IV non–small cell lung cancer. Univariate and multivariate analyses were performed to determine the effects of histological type on progression-free survival and response rates. Results: On pooled analysis of the data, according to histological type, median progression-free survival was 3.8 months in patients with squamous cell carcinoma and 4.4 months in those with non-squamous cell carcinoma. Both analyses showed that progression-free survival and response rate did not differ significantly. Conclusion: Unlike molecular targeted agents and pemetrexed, a combination of cisplatin and S-1 may be no difference in response according to histological type.
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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:52:43 | 显示全部楼层 来自: 浙江温州
S-1 monotherapy for previously treated non-small cell lung cancer: A retrospective analysis by age and histopathological type 7 P$ h. H- \' c5 y4 e
* \, S% Y; j: Q  h
Authors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato
1 e- y# b3 `$ m- v+ M
6 [7 G* p  N6 }' U( ~0 Y3 VAffiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  4 d% A+ X5 _- P. i( M+ G# e; W( J6 P

+ d' P% I7 p; HPublished online on: Thursday, December 1, 2011 9 e7 A1 s& q, _+ V- s; e7 N3 r/ W

" g! F' @. x: y' s( }0 ^Doi: 10.3892/ol.2011.507
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5 e: T& f, T! X; bPages: 405-410 , t5 F& n( o* z( ^" `$ [
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Abstract:$ b9 W& v, G8 U
S-1, an oral fluoropyrimidine derivative, has been approved for the treatment of non-small cell lung cancer (NSCLC) in Japan. In the present study, the efficacy and safety of S-1 monotherapy for elderly patients with previously treated NSCLC were retrospectively evaluated, and the efficacy of S-1 monotherapy was compared by histopathological type. This retrospective study included 54 patients with advanced or recurrent NSCLC who had received S-1 monotherapy following the failure of previous chemotherapy regimens at our institutes. Patient outcomes were compared based on their age and histopathological type. S-1 was administered orally, twice daily, while the duration and interval were modified according to the medical condition of each patient. The default delivery schedule, the mean number of S-1 cycles, did not differ significantly between the two age groups (<70 and ≥70 years). The rate of therapy discontinuation, schedule modification or dose reduction due to intolerable toxicities or patient refusal was relatively frequent in the older group (40.7 and 55.6% for ages <70 and ≥70 years, respectively; p=0.414), and the incidence of grade 3 anemia was relatively high in the older group (3.7 and 18.5%, respectively; p=0.192). The response rates (13.0 and 4.8%, respectively; p=0.609) and disease control rates (39.1 and 33.3%, respectively; p=0.761) did not differ significantly between the two age groups. According to histopathological type, the disease control rate was significantly higher in adenocarcinoma (57.9%) compared to non-adenocarcinoma (20.0%, p=0.013). Thus, S-1 monotherapy may be equally effective and tolerated in patients <70 years and those ≥70 years. Additionally, adenocarcinoma may have a higher disease control rate than non-adenocarcinoma.
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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:57:27 | 显示全部楼层 来自: 浙江温州
Thymidylate synthase (TS) gene expression in primary lung cancer patients: a large-scale study in Japanese population$ v9 E. M1 h+ h0 b& `
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
' @, F; |) @3 Z" Z0 l+ Author Affiliations  l' [1 Q& B$ I, R
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
- v+ N" a# Q9 L0 N& ?% o% `2Department of Thoracic Surgery, Kyoto University, Kyoto
( q, l+ _  Z7 m; [9 \' L2 z& Q  ^3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
- p1 m: [/ H3 |6 B9 c, x&#8629;*Correspondence to: Dr F. Tanaka, Second Department of Surgery, University of Environmental and Occupational Health, 1-1 Isegaoka, Yahata-nishi, Kitakakyushu, 807-8555, Japan. Tel: +81-93-891-7442; Fax: +81-93-692-4004; E-mail: ftanaka@med.uoeh-u.ac.jp 1 |1 ^2 f" t' |- C0 k4 _. ]
Received September 3, 2010. % A( q  H* [1 J9 @! ~: \5 j
Revision received November 11, 2010.
- ]# u* w2 f9 J3 S3 V& ~Accepted November 17, 2010.
$ k' _4 J) C- F' KAbstract7 p8 D2 f, Q; u  _
Background: Previous small-sized studies showed lower thymidylate synthase (TS) expression in adenocarcinoma of the lung, which may explain higher antitumor activity of TS-inhibiting agents such as pemetrexed.
/ D! q  ~5 N+ t8 J/ U9 tPatients and methods: To quantitatively measure TS gene expression in a large-scale Japanese population (n = 2621) with primary lung cancer, laser-captured microdissected sections were cut from primary tumors, surrounding normal lung tissues and involved nodes.
1 r/ i1 f4 C: j6 L3 JResults: TS gene expression level in primary tumor was significantly higher than that in normal lung tissue (mean TS/β-actin, 3.4 and 1.0, respectively; P < 0.01), and TS gene expression level was further higher in involved node (mean TS/β-actin, 7.7; P < 0.01). Analyses of TS gene expression levels in primary tumor according to histologic cell type revealed that small-cell carcinoma showed highest TS expression (mean TS/β-actin, 13.8) and that squamous cell carcinoma showed higher TS expression as compared with adenocarcinoma (mean TS/β-actin, 4.3 and 2.3, respectively; P < 0.01); TS gene expression was significantly increased along with a decrease in the grade of tumor cell differentiation. There was no significant difference in TS gene expression according to any other patient characteristics including tumor progression.
/ w" e+ S6 [. a1 lConclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. ( F+ `. P. G5 A$ V$ |4 [9 k
个人公众号:treeofhope
走在异乡  高中一年级 发表于 2012-4-28 00:30:22 | 显示全部楼层 来自: 四川成都
一直关注老马的帖子,前方的指明灯。祝福你爸好疗效
累计签到:1 天
连续签到:1 天
[LV.1]初来乍到
baiselianyi  初中二年级 发表于 2012-4-28 10:24:44 | 显示全部楼层 来自: 浙江台州
一直得到老马帮助,祝福老马爸爸
老马  博士一年级 发表于 2012-4-28 18:00:37 | 显示全部楼层 来自: 浙江温州
26日吃了12片地米(0.75mg一片),27日吃了22片地米(0.75mg 一片),28日吃了12片地米(0.75mg一片),都分二次吃。
$ g9 g! c. U# h# T. |2 y# Q& ^今天为止没有任何反应,每天吃VC,VB2,还有漱口水,就怕口腔溃疡。
个人公众号:treeofhope
bishop_cn  大学一年级 发表于 2012-4-28 23:16:11 | 显示全部楼层 来自: 中国
副作用如何,单药反应很小吧?
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老马  博士一年级 发表于 2012-4-29 00:20:00 | 显示全部楼层 来自: 浙江温州
LUX-Lung 8: A Phase III Trial of Afatinib (BIBW 2992) Versus Erlotinib for the Treatment of Squamous Cell Lung Cancer After at Least One Prior Platinum Based Chemotherapy
. _; o6 P8 p% ^$ T" ehttp://clinicaltrials.gov/ct2/show/NCT015235872 Y: V' @; F% f4 V( N5 t
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BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
5 R- i9 L2 t% d6 G+ G0 F7 n  ehttp://clinicaltrials.gov/ct2/show/NCT01156545
个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-29 20:53:58 | 显示全部楼层 来自: 浙江温州
本帖最后由 老马 于 2012-4-30 09:33 编辑 7 c3 c) {2 i8 Q2 q, k7 c8 S- t+ ~
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从4月24日开始到4月28日,打了5天的舒普深(注射用头孢哌酮钠舒巴坦钠),效果非常好。
9 |* H2 c5 h! A. Y/ H- }. B至今为止,未出现化疗副作用。
个人公众号:treeofhope
英雄武松  大学四年级 发表于 2012-4-30 01:37:05 | 显示全部楼层 来自: 哈萨克斯坦
老马 发表于 2012-4-29 20:53
9 }- p. p' e: x/ {/ B( \2 e从4月24日开始到4月28日,打了5天的打了5天舒普深(注射用头孢哌酮钠舒巴坦钠),效果非常好。+ W+ X. p- I7 V3 I* w! G& j
至今为止,未出 ...
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没有副作用是第一追求,效果显著是第二追求。
; M- C5 O* {; `! n+ Z& S% D不错。

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